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    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • View similar jobs with this employer
    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • View similar jobs with this employer
    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • View similar jobs with this employer
    • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • View similar jobs with this employer
    • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
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    • You have successfully managed multiple clinical trial protocols across diverse investigative sites.
    • IQVIA has access to significant data pools allowing better…
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    • Assist clinical staff members in various clinical activities as required.
    • Provision of medical care and oversight of clinical trial participants.
    • Duties will also include sample preparation, the routine operation, maintenance and troubleshooting of laboratory instrumentation, technical validation and…
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    • Assist clinical staff members in various clinical activities as required.
    • Provision of medical care and oversight of clinical trial participants.
    • Assist clinical staff members in various clinical activities as required.
    • Previous clinical research experience in SMO/CRO.
    • 2+ years of psychiatry experience.
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    • At least 5 years’ clinical experience with at least 2 years in the NHS.
    • Ensuring all clinical trials are conducted according to Protocol, recruiting patients…
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    • Assist clinical staff members in various clinical activities as required.
    • Provision of medical care and oversight of clinical trial participants.
    • Familiarity with traditional performance metrics of clinical diagnostic tools.
    • Stay abreast of industry and academic developments in the Statistical Genomics,…
    • To principal scientist level, developing both direct reports and matrixed team.
    • To those interested in this position, the position office will based in Chengdu…
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    • Delivers clinical safety input into clinical development program.
    • Ability to independently search clinical safety and literature databases for relevant…

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